rs9499708

Orientation

plus

Stabilized

plus

Make rs9499708(C;C)

Make rs9499708(C;T)

Make rs9499708(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

103997492

is a	snp
is	mentioned by
dbSNP	rs9499708
dbSNP (classic)	rs9499708
ClinGen	rs9499708
ebi	rs9499708
HLI	rs9499708
Exac	rs9499708
Gnomad	rs9499708
Varsome	rs9499708
LitVar	rs9499708
Map	rs9499708
PheGenI	rs9499708
Biobank	rs9499708
1000 genomes	rs9499708
hgdp	rs9499708
ensembl	rs9499708
geneview	rs9499708
scholar	rs9499708
google	rs9499708
pharmgkb	rs9499708
gwascentral	rs9499708
openSNP	rs9499708
23andMe	rs9499708
SNPshot	rs9499708
SNPdbe	rs9499708
MSV3d	rs9499708
GWAS Ctlg	rs9499708

GMAF

0.258

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 22889921]
Trait	Obsessive-compulsive disorder
Title	Genome-wide association study of obsessive-compulsive disorder.
Risk Allele
P-val	3E-6
Odds Ratio	1.20 NR